A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10526n54



Internal ID22778421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32517715..32556447hg38UCSC Ensembl
chr6:32485492..32524224hg19UCSC Ensembl
chr6:32593470..32632202hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3838733
hg1938733
hg1838733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602402, nsv602415, nsv602400, nsv602401, nsv602422
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10526n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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